Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 73950-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Miniso Depot Ca, Inc. for the product Hand Sanitizer (NDC 73950-005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - stop use, storage and handling, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Uses Decrease bacteria on hands
Warnings
Warnings For external use only.
Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Otc - Keep Out Of Reach Of Children
Keep it out of reach of children.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop.If swallowed,get medical help or contact a doctor right away.
Storage And Handling
Storage: Flammable,Avoid direct sunlight and keep away from fire.
Dosage & Administration
Directions: Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredient
Inactive Ingredients:
Water, Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Fragrance, Acrylates/C10-30 AlkyI Acrylate Crosspolymer, Aminomethyl Propanol, Maltodextrin.
Package Label.Principal Display Panel
Image Of Bottle Label (Bg)
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